Sexual dimorphism in developmental programming of the bovine preimplantation embryo caused by colony-stimulating factor 2

Biol Reprod. 2014 Sep;91(3):80. doi: 10.1095/biolreprod.114.121087. Epub 2014 Jul 30.

Abstract

Physiology of the adult can be modified by alterations in prenatal development driven by the maternal environment. Developmental programming, which can be established before the embryo implants in the uterus, can affect females differently than males. The mechanism by which sex-specific developmental programming is established is not known. Here we present evidence that maternal regulatory signals change female embryos differently than male embryos. In particular, actions of the maternally derived cytokine CSF2 from Day 5 to Day 7 of development affected characteristics of the embryo at Day 15 differently for females than males. CSF2 decreased length and IFNT secretion of female embryos but increased length and IFNT secretion of male embryos. Analysis of a limited number of samples indicated that changes in the transcriptome and methylome caused by CSF2 also differed between female and males. Thus, sex-specific programming by the maternal environment could occur when changes in secretion of maternally derived regulatory molecules alter development of female embryos differently than male embryos.

Keywords: DNA methylation; bovine; colony-stimulating factor 2; cytokines; early development; embryo; epigenetics; gene expression; sex; transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Inbred Strains
  • Blastocyst / metabolism*
  • Cattle
  • Ectogenesis
  • Embryo Culture Techniques
  • Embryo Transfer
  • Embryonic Development*
  • Endometrium / metabolism*
  • Female
  • Fertilization in Vitro
  • Gene Expression Regulation, Developmental*
  • Interferon Type I / metabolism*
  • Interleukin-3 / genetics
  • Interleukin-3 / metabolism*
  • Male
  • Maternal-Fetal Exchange*
  • Methylation
  • Pregnancy
  • Pregnancy Proteins / metabolism*
  • Protein Processing, Post-Translational
  • Random Allocation
  • Recombinant Proteins / metabolism
  • Sex Characteristics

Substances

  • Interferon Type I
  • Interleukin-3
  • Pregnancy Proteins
  • Recombinant Proteins
  • interferon tau

Associated data

  • GEO/GSE55364